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Tolerability of Velcade (Bortezomib) subcutaneous administration using a maximum volume of 3 mL per injection site.
Ng, Pamela; Incekol, Diana; Lee, Roy; Paisley, Emma; Dara, Celina; Brandle, Ian; Kaufman, Marina; Chen, Christine; Trudel, Suzanne; Tiedemann, Rodger; Reece, Donna; Kukreti, Vishal.
Afiliação
  • Ng P; Dept. of Pharmacy, Princess Margaret Cancer Centre, UHN Toronto, ON Pamela.Ng@uhn.ca.
  • Incekol D; Dept. of Nursing, Princess Margaret Cancer Centre, UHN, Toronto, ON.
  • Lee R; Dept. of Pharmacy, Princess Margaret Cancer Centre, UHN Toronto, ON.
  • Paisley E; Dept. of Nursing, Princess Margaret Cancer Centre, UHN, Toronto, ON.
  • Dara C; Dept. of Pharmacy, Princess Margaret Cancer Centre, UHN Toronto, ON.
  • Brandle I; Dept. of Nursing, Princess Margaret Cancer Centre, UHN, Toronto, ON.
  • Kaufman M; Dept. of Nursing, Princess Margaret Cancer Centre, UHN, Toronto, ON.
  • Chen C; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, UHN, Toronto, ON.
  • Trudel S; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, UHN, Toronto, ON.
  • Tiedemann R; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, UHN, Toronto, ON.
  • Reece D; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, UHN, Toronto, ON.
  • Kukreti V; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, UHN, Toronto, ON.
J Oncol Pharm Pract ; 21(4): 285-92, 2015 Aug.
Article em En | MEDLINE | ID: mdl-24781451
ABSTRACT
Subcutaneous injection is now commonly used as a standard for bortezomib administration. The bortezomib (Velcade(®)) product monograph recommends that intravenous injections be prepared at a concentration of 1 mg/mL, while subcutaneous injections may be prepared at a concentration of 2.5 mg/mL. Many institutions and subcutaneous administration guidelines use 2 mL as the maximum volume for subcutaneous injection. Using 2 mL as the maximum volume for injection would mean that many patients receiving bortezomib will receive two injections during each visit with common dosing parameters. In this prospective study evaluating a change to subcutaneous administration, bortezomib 1 mg/mL was administered subcutaneously at a higher maximum of 3 mL per injection site. For 57 individual patients, 339 doses were administered. Skin reactions were noted in 42% with all reactions being Grade 1 or 2. Patients tolerated subcutaneous injections well and only four patients were switched back to intravenous route. This is the first time that subcutaneous bortezomib of a volume up to a maximum of 3 mL (bortezomib 3 mg) per injection site has been reported. This higher single dose is well tolerated with limited skin reactions, no significant hypotension and facilitates ease of administration with only 5 patients needing two injections per visit. If the maximum volume for injection was kept at 2 mL, a total of 46 patients would have received two injections per visit.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bortezomib / Antineoplásicos Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bortezomib / Antineoplásicos Idioma: En Ano de publicação: 2015 Tipo de documento: Article